Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Micardis Tablets Recalled by Boehringer Ingelheim Pharmaceuticals, Inc. Due to Subpotent Drug
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Boehringer Ingelheim Pharmaceuticals, Inc. directly.
Affected Products
Micardis Tablets, (telmisartan Tablets) 80 mg, 30 ct. per folding cartons, Rx only, NDC 0597-0041-37), Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877
Quantity: 15,198 bottles (30 tablets per bottle)
Why Was This Recalled?
Subpotent Drug
Where Was This Sold?
This product was distributed to 10 states: AR, CO, CT, LA, NH, NJ, NC, ND, OH, PA
About Boehringer Ingelheim Pharmaceuticals, Inc.
Boehringer Ingelheim Pharmaceuticals, Inc. has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report